✦ LIBER ✦

The biological functions of the methyl-CpG-binding protein MeCP2 and its implication in Rett syndrome

✍ Scribed by Xinsheng Nan; Adrian Bird

Book ID: 117545546
Publisher: Elsevier Science
Year: 2001
Tongue: English
Weight: 133 KB
Volume: 23
Category: Article
ISSN: 0387-7604
DOI: 10.1016/s0387-7604(01)00333-3

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Patho-Epigenetics of Disease || Dysfunct

Patho-Epigenetics of Disease || Dysfunction of the Methyl-CpG-Binding Protein MeCP2 in Rett Syndrome

✍ Minarovits, Janos; Niller, Hans Helmut 📂 Article 📅 2012 🏛 Springer New York ⚖ 306 KB

Methyl-CpG binding protein 2 gene (MECP2

Methyl-CpG binding protein 2 gene (MECP2) variations in Japanese patients with Rett syndrome: pathological mutations and polymorphisms

✍ Takayuki Fukuda; Yushiro Yamashita; Shinichiro Nagamitsu; Kenichi Miyamoto; Jing 📂 Article 📅 2005 🏛 Elsevier Science 🌐 English ⚖ 154 KB

Mutations in the gene encoding methyl-Cp

Mutations in the gene encoding methyl-CpG-binding protein 2 cause Rett syndrome

✍ Ignatia B. Van den Veyver; Huda Y. Zoghbi 📂 Article 📅 2001 🏛 Elsevier Science 🌐 English ⚖ 132 KB

Mutation analysis of the methyl-CpG-bind

Mutation analysis of the methyl-CpG-binding protein 2 gene (MECP2) in Rett patients with preserved speech

✍ Yushiro Yamashita; Ikuko Kondo; Takayuki Fukuda; Riyo Morishima; Akira Kusaga; R 📂 Article 📅 2001 🏛 Elsevier Science 🌐 English ⚖ 64 KB

Binding of the Rett syndrome protein, Me

Binding of the Rett syndrome protein, MeCP2, to methylated and unmethylated DNA and chromatin

✍ Jeffrey C. Hansen; Rajarshi P. Ghosh; Christopher L. Woodcock 📂 Article 📅 2010 🏛 John Wiley and Sons 🌐 English ⚖ 144 KB

Methylated CpG Binding Protein 2 (MeCP2) is a nuclear protein named for its ability to selectively recognize methylated DNA. Much attention has been focused on understanding MeCP2 structure and function in the context of its role in Rett syndrome, a severe neurodevelopmental disorder that afflicts o

Mutations and polymorphisms in the human

Mutations and polymorphisms in the human methyl CpG-binding protein MECP2

✍ Gabriel Miltenberger-Miltenyi; Franco Laccone 📂 Article 📅 2003 🏛 John Wiley and Sons 🌐 English ⚖ 188 KB

Rett syndrome (RTT or RS) is a neurodevelopmental disorder and one of the most frequent genetic diseases in girls. Mutations of the MECP2 gene have been found in a variety of different RTT phenotypes. The MECP2 gene (Xq28) has been described in 1992. Up to now, 218 different mutations have been repo